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See today's BioWorldSee today's BioWorld Asia
Home » HLB's Elevar subsidiary confirms FDA to review rivoceranib by 2024
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HLB's Elevar subsidiary confirms FDA to review rivoceranib by 2024

July 18, 2023
By Marian (YoonJee) Chu
Elevar Therapeutics Inc. said that the U.S. FDA accepted its NDA for oral tyrosine kinase inhibitor rivoceranib in combination with PD-1 inhibitor camrelizumab (Airuika) as a first-line treatment for liver cancer. The FDA stamped an official PDUFA target action date of May 16, 2024.
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